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  • risk premia  (2)
  • Analytical Chemistry and Spectroscopy  (1)
  • Azulenones, cis-octa- and decahydro-  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Interest expectations and exchange rates news (1998)
    Springer
    Empirical economics 23 (1998), S. 525-534 
    Details
    ISSN: 1435-8921
    Keywords: Key words: Exchange rates ; risk premia ; survey data ; JEL classification: F31
    Source: Springer Online Journal Archives 1860-2000
    Topics: Economics
    Notes: Abstract. Using a new survey data set of matched exchange rate and interest rate expectations for eight currencies relative to the German mark, we examine empirically the relationship between exchange rate returns, `news' and risk premia. “News” on interest differentials enters significantly in equations for the difference between the spot rate and the lagged forward rate for the British pound, Japanese yen, Spanish peseta and the US dollar. An unexpected rise in the interest rate differential tends to strengthen the domestic exchange rate. For each of these currencies, we also find significant effects of our ex-ante measure of the risk premium. In addition, we investigate the effect of lagged interest rate differentials as proxy for the risk premium and find that they do not capture time-varying risk premia as is widely suggested in the literature, but probably capture a peso-problem, learning about a policy change, a market-inefficiency or a combination of these factors.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s001810050034
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Interest expectations and exchange rates news (1998)
    Springer
    Empirical economics 23 (1998), S. 525-534 
    Details
    ISSN: 1435-8921
    Keywords: Exchange rates ; risk premia ; survey data ; F31
    Source: Springer Online Journal Archives 1860-2000
    Topics: Economics
    Notes: Abstract Using a new survey data set ofmatched exchange rate and interest rate expectations for eight currencies relative to the German mark, we examine empirically the relationship between exchange rate returns, ‘news’ and risk premia. “News” on interest differentials enters significantly in equations for the difference between the spot rate and the lagged forward rate for the British pound, Japanese yen, Spanish peseta and the US dollar. An unexpected rise in the interest rate differential tends to strengthen the domestic exchange rate. For each of these currencies, we also find significant effects of our ex-ante measure of the risk premium. In addition, we investigate the effect of lagged interest rate differentials as proxy for the risk premium and find that they do not capture time-varying risk premia as is widely suggested in the literature, but probably capture a peso-problem, learning about a policy change, a market-inefficiency or a combination of these factors.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01205992
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Synthese mittlerer und großer Ringe, XXXV[1]. Funktionalisierte Hydroazulenone durch transannulare Cyclisierungen von 10-Oxo-3,6-hexanooxepin-4,5-dicarbonsäure-dimethylester (1993)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2691-2696 
    Details
    ISSN: 0009-2940
    Keywords: Azulenones, cis-octa- and decahydro- ; Stereoselective cyclization ; Hydrogenation ; Oxidation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of Medium and Large Rings, XXXV[1]. - Functionalized Hydroazulenones by Transannular Cyclizations of Dimethyl 10-Oxo-3,6-hexanooxepine-4,5-dicarboxylateTwo differently bridged hydroazulenones 2 and 3 are obtained in 69 and 61% yield, respectively, by treatment of the title compound 1 with sodium methoxide. The course of these intramolecular transannular cyclizations strongly depends on the amount of added base. 2 is hydrogenated to the ketones 9 and 10. Oxidative cleavage of the enol ether double bond of 3 and 10 leads to the octahydroazulene-1,6-dione 11 and to the decahydroazulene-3,8-dione 12, respectively.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19931261219
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Chirality in hindered naphthylamines (1988)
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 26 (1988), S. 608-611 
    Details
    ISSN: 0749-1581
    Keywords: Chirality ; Chiral auxiliaries ; Napthylamines ; Steric hindrance ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: peri-Substituted ethylmethyl-1-naphthylamines were shown by means of 1H and 13C NMR spectroscopy to be chiral at and above room temperature.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/mrc.1260260714
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    Paper (German National Licenses)
    Fulltext
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